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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 6
2004 2
2005 3
2006 1
2007 2
2008 3
2009 1
2010 1
2011 5
2012 1
2013 5
2014 3
2016 1
2018 3
2019 2
2020 4
2021 4
2022 2
2023 2
2024 0

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48 results

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Page 1
Muscular dystrophies due to glycosylation defects.
Muntoni F, Torelli S, Brockington M. Muntoni F, et al. Among authors: torelli s. Neurotherapeutics. 2008 Oct;5(4):627-32. doi: 10.1016/j.nurt.2008.08.005. Neurotherapeutics. 2008. PMID: 19019316 Free PMC article. Review.
Defective glycosylation in muscular dystrophy.
Muntoni F, Brockington M, Blake DJ, Torelli S, Brown SC. Muntoni F, et al. Among authors: torelli s. Lancet. 2002 Nov 2;360(9343):1419-21. doi: 10.1016/S0140-6736(02)11397-3. Lancet. 2002. PMID: 12424008 Review.
Defective glycosylation in congenital muscular dystrophies.
Muntoni F, Brockington M, Torelli S, Brown SC. Muntoni F, et al. Among authors: torelli s. Curr Opin Neurol. 2004 Apr;17(2):205-9. doi: 10.1097/00019052-200404000-00020. Curr Opin Neurol. 2004. PMID: 15021250 Review.
POMK regulates dystroglycan function via LARGE1-mediated elongation of matriglycan.
Walimbe AS, Okuma H, Joseph S, Yang T, Yonekawa T, Hord JM, Venzke D, Anderson ME, Torelli S, Manzur A, Devereaux M, Cuellar M, Prouty S, Ocampo Landa S, Yu L, Xiao J, Dixon JE, Muntoni F, Campbell KP. Walimbe AS, et al. Among authors: torelli s. Elife. 2020 Sep 25;9:e61388. doi: 10.7554/eLife.61388. Elife. 2020. PMID: 32975514 Free PMC article.
Investigating the role of dystrophin isoform deficiency in motor function in Duchenne muscular dystrophy.
Chesshyre M, Ridout D, Hashimoto Y, Ookubo Y, Torelli S, Maresh K, Ricotti V, Abbott L, Gupta VA, Main M, Ferrari G, Kowala A, Lin YY, Tedesco FS, Scoto M, Baranello G, Manzur A, Aoki Y, Muntoni F. Chesshyre M, et al. Among authors: torelli s. J Cachexia Sarcopenia Muscle. 2022 Apr;13(2):1360-1372. doi: 10.1002/jcsm.12914. Epub 2022 Jan 26. J Cachexia Sarcopenia Muscle. 2022. PMID: 35083887 Free PMC article.
Dystrophin quantification: Biological and translational research implications.
Anthony K, Arechavala-Gomeza V, Taylor LE, Vulin A, Kaminoh Y, Torelli S, Feng L, Janghra N, Bonne G, Beuvin M, Barresi R, Henderson M, Laval S, Lourbakos A, Campion G, Straub V, Voit T, Sewry CA, Morgan JE, Flanigan KM, Muntoni F. Anthony K, et al. Among authors: torelli s. Neurology. 2014 Nov 25;83(22):2062-9. doi: 10.1212/WNL.0000000000001025. Epub 2014 Oct 29. Neurology. 2014. PMID: 25355828 Free PMC article.
High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients.
Torelli S, Scaglioni D, Sardone V, Ellis MJ, Domingos J, Jones A, Feng L, Chambers D, Eastwood DM, Leturcq F, Yaou RB, Urtizberea A, Sabouraud P, Barnerias C, Stojkovic T, Ricci E, Beuvin M, Bonne G, Sewry CA, Willis T, Kulshrestha R, Tasca G, Phadke R, Morgan JE, Muntoni F. Torelli S, et al. J Neuropathol Exp Neurol. 2021 Oct 26;80(10):955-965. doi: 10.1093/jnen/nlab088. J Neuropathol Exp Neurol. 2021. PMID: 34498054 Free PMC article.
48 results